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United States · US · US:71335-1187_c93fa349-242e-4268-a6d5-0db5564cc181

Escitalopram

Orange BookUNIISPLATC N06AB10

Last synced from FDA National Drug Code directory (United States) on

Identification

ManufacturerBryant Ranch Prepack
CountryUS (United States)
ATC codeN06AB10
Dispensing
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 9

  • ndc11
    7133511871
    30 TABLET, FILM COATED in 1 BOTTLE (71335-1187-1)
  • ndc11
    7133511872
    28 TABLET, FILM COATED in 1 BOTTLE (71335-1187-2)
  • ndc11
    7133511873
    60 TABLET, FILM COATED in 1 BOTTLE (71335-1187-3)
  • ndc11
    7133511874
    90 TABLET, FILM COATED in 1 BOTTLE (71335-1187-4)
  • ndc11
    7133511875
    10 TABLET, FILM COATED in 1 BOTTLE (71335-1187-5)
  • ndc11
    7133511876
    120 TABLET, FILM COATED in 1 BOTTLE (71335-1187-6)
  • ndc11
    7133511877
    7 TABLET, FILM COATED in 1 BOTTLE (71335-1187-7)
  • ndc11
    7133511878
    180 TABLET, FILM COATED in 1 BOTTLE (71335-1187-8)
  • ndc11
    7133511879
    100 TABLET, FILM COATED in 1 BOTTLE (71335-1187-9)

Annotations

UNII (FDA Substance ID)
5U85DBW7LO
ESCITALOPRAM OXALATE
RxCUI 353108
Orange Book
A078032
ABABAB
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
  "unii": {
    "unii": "5U85DBW7LO",
    "rxcui": "353108",
    "inchikey": "KTGRHKOEFSJQNS-BDQAORGHSA-N",
    "display_name": "ESCITALOPRAM OXALATE",
    "substance_type": "chemical",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "spl_meta": {
    "43eb9e4f-1a46-46f7-9e9d-43e866963b37": {
      "match": "brand_token",
      "title": "ESCITALOPRAM TABLET, FILM COATED [BRYANT RANCH PREPACK]",
      "spl_version": "104",
      "published_date": "2026-06-01"
    }
  },
  "productid": "71335-1187_c93fa349-242e-4268-a6d5-0db5564cc181",
  "productndc": "71335-1187",
  "dosage_form": "TABLET, FILM COATED",
  "orange_book": {
    "appl_no": "078032",
    "products": [
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "EQ 5MG BASE",
        "product_no": "001",
        "approval_date": "Aug 28, 2015"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "EQ 10MG BASE",
        "product_no": "002",
        "approval_date": "Aug 28, 2015"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "EQ 20MG BASE",
        "product_no": "003",
        "approval_date": "Aug 28, 2015"
      }
    ],
    "appl_type": "A"
  },
  "dea_schedule": null,
  "product_type": "HUMAN PRESCRIPTION DRUG",
  "substance_name": "ESCITALOPRAM OXALATE",
  "proprietary_name": "Escitalopram",
  "active_ingred_unit": "mg/1",
  "application_number": "ANDA078032",
  "marketing_category": "ANDA",
  "nonproprietary_name": "Escitalopram",
  "start_marketing_date": "20160201",
  "active_numerator_strength": "10"
}

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